Package 68382-096-01

{"route": ["ORAL"], "spl_id": "8b9ea8e4-c27b-4b81-b8d0-2d5eddcec21a", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["805a1acd-2e0d-48f1-af6b-0e5d8e06c228"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-096-01)", "package_ndc": "68382-096-01", "marketing_start_date": "20080103"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68382-096-05)", "package_ndc": "68382-096-05", "marketing_start_date": "20080103"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68382-096-77)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-096-30)", "package_ndc": "68382-096-77", "marketing_start_date": "20080103"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "68382-096_8b9ea8e4-c27b-4b81-b8d0-2d5eddcec21a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "68382-096", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040657", "marketing_category": "ANDA", "marketing_start_date": "20080103", "listing_expiration_date": "20261231"}